| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:231706148-231706670 | Common:8; Rare:269 | ||||
| chr2:231706831-231707632 | Common:3; Rare:610 | ||||
| chr2:231708221-231709031 | Common:13; Rare:949 | ||||
| chr2:231709231-231709436 | Common:4; Rare:84 | ||||
| chr2:231709348-231709956 | Common:14; Rare:460 | ||||
| chr2:231709970-231710120 | Common:3; Rare:81 | ||||
| chr2:231710218-231710645 | Common:26; Rare:954 | ||||
| chr2:231711219-231712100 | Common:9; Rare:720 | ||||
| chr2:231781051-231781824 | Common:20; Rare:789 | ||||
| chr2:231781906-231782306 | Rare:116 | ||||
| chr2:231786150-231786510 | Common:7; Rare:259 | ||||
| chr2:231786720-231787080 | Rare:98 | ||||
| chr2:231961141-231961545 | Common:5; Rare:148 | ||||
| chr2:231961555-231961781 | Rare:354; Clinvar:19 | ||||
| chr2:231961830-231962065 | Common:1; Rare:73 |